4 Qa Auditor Jobs

At Jubilant FoodWorks, we believe in a world powered by simplicity, flavour, and cutting-edge technology. We are the first in the industry to incorporate AI, IoT, and breakthroughs that push the envelope to author food-tech innovations. Trusted by global brands like Dominos Pizza, Dunkin (Coffee & Donuts), and Popeyes (Fried Chicken), we curate the best blend of food and technology for our consumers. We are powered by customer insights, striving today for a better tomorrow. Anchored by ambitions and a collective of believers, we are tempered by transparency and believe in growing together. We are dynamic and tech-driven, valuing each other's ideas. A marriage of two worlds - Food & Tech. At Jubilant FoodWorks, careers are carved to achieve milestones not just for the company but also for YOU. Come be a part of the FoodTech Powerhouse and shape the future of food and technology. We are looking for a Food Technology person for the role of QA auditor (support). This position may require travel. The salary offered is as per company norms. Freshers are welcome to apply for this exciting opportunity. If you are interested, please send your application to harishkumar.dhakate@jublfood.com. Join us in creating innovative solutions at the intersection of food and technology.,

QA Auditor

Knowledge of maintaining agricultural produce To maintain standards and specifications of all raw materials and finished products To assist in all areas related to product quality including troubleshooting, visiting, production, facilities, designing, training, quality control panel To provide information that is accurate, reliable and adequate for the intended purpose Keep the management team apprised of the quality issues Responsible for inspecting and documenting all incoming fruit, vegetables, packaging materials, and ensure all product quality standards are adhered to. Perform routine quality and condition inspections on existing inventory to assist in first-in, first-out (FIFO) or worst-in, first-out (WIFO) stock rotation. Ensure all inbound carrier trailers and materials meet company quality and food safety standards. Communicate Quality Assurance issues, including defect levels and problem loads, to Sales, Production, and QA managers. Verify customer specifications, quality requirements of product orders, documentation submitted and approved vendors. Coordinate inspections Maintain instruments, records of calibrations, and supplies as needed to meet quality inspection requirements to ensure that company standards are met. Work closely with Production and Warehouse departments to ensure effective stock rotation to reduce shrinkage. Maintain daily inbound inspection and defect reports , weekly inbound raw material reports and keeps accurate documentation for food safety purposes. Responsible for daily sanitation of equipment, and inspect repack products as needed. Ensure quality of product meets quality standards and communicate any inconsistency to sales, purchasing, management, and quality control department.

At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Core Purpose of the Role : To perform the role as Clinical QA auditor to verify compliance to ICH-GCP, NDCT Rule and other applicable regulatory requirements with respect to BABE/ Phase I studies. Comfortable working and communicating professionally with others to reach understanding and agreement as necessary. Other Responsibilities: To perform or assist any other relevant job with relevant training as and when required by Department Head or Management. Role Accountabilities: To perform study specific in-process audits as per audit plan to ensure that study is conducted in compliance with in-house SOPs, protocol and applicable regulatory guidelines etc., To perform study specific retrospective audits of informed consent document, study files like TMF, case report forms, raw data forms, draft clinical study report and other applicable documents to ensure that study is conducted in compliance with in-house SOPs, protocol and applicable regulatory guidelines etc., To perform database audits in EDC application for applicable studies. To prepare and issue audit reports to respective operations team in consultation with Manager/ Department Head and follow-up the implementation of CAPA to ensure timely closure of audit observations. To initiate change control and follow-up for the same for timely closure in consultation with Manager/ Department Head. To review change control, deviation and other QMS elements taken by operations team and follow-up for its timely closure. To review draft documents like Protocol, ICD, CRF etc., before its finalization. To assist for system audit as co-auditor and or providing input to Compliance QA team, if required. To perform vendor audit as lead/ co-auditor as per vendor audit forecast plan, if required. To review qualification and validation documents, if required by Manager/ Department Head. To assist and or participate whenever required as per Department Head discretion during system audit, internal and external audits and inspection as part of audit/ inspection readiness. To assist in preparation or reviewing the CAPA whenever required during system audit, internal and external audits and inspection. To ensure QA records generated are archived on periodic basis. To assist Manager/ Department Head whenever required to collate quality systems data for trending the Quality metrics. To escalate immediately to Manager/ Department Head in case of any serious non-compliance to protocol and ALCOA+ principles. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role 1. Experience: 6 - 9 years 2. Demonstrated Capability: Auditing skills, Understanding of regulations & Attention to detail 3. Education: M.Sc., in Life Sciences or M. Pharm., 4. Sound technical Knowledge in ICH GCP, NDCT Rule and other applicable guidelines.